Scientist

• Develop preclinical testing strategies supporting product development, regulatory submissions, and clinical translation
• Design in vivo studies evaluating device safety, functionality, performance, and clinical relevance
• Select animal models, study endpoints, controls, and evaluation methods based on intended use and regulatory expectations
• Ensure study objectives address product risks, design questions, and performance claims
• Act as study sponsor representative for external CRO and research site activities
• Prepare study protocols, technical justifications, study reports, technical assessments, and regulatory documentation
• Oversee study conduct for regulatory, GLP, and animal welfare compliance
• Analyze and interpret preclinical data and study reports
• Identify risks, failure modes, and design improvement opportunities
• Monitor regulatory guidance and drive continuous improvement in preclinical methodologies and study designs
• Partner with R&D, Clinical, Regulatory Affairs, Biocompatibility, Toxicology, Quality, and Marketing teams across multiple projects
• Provide consultative direction and technical guidance to support high-quality product development
• Support regulatory authority interactions with scientific rationale and study interpretations
• Manage prioritization and communicate resource needs and project updates to the PMO and Manager
• Drive proactive risk resolution with team members, peers, PMO, and management
• May lead groups and supervise direct reports or contractors
• Mentor junior scientists
• Represent the company in regulatory meetings, conferences, standards committees, or industry consortia
• Communicate business-related issues or opportunities to the next management level
• Follow and ensure compliance with applicable Health, Safety and Environmental practices, regulations, policies, and procedures

Staff Preclinical Scientist advancing Johnson & Johnson MedTech device safety through in vivo research

Staff Preclinical Scientist

Staff Preclinical Scientist designing and interpreting in vivo studies for Johnson & Johnson MedTech devices.
Supporting safety, regulatory submissions, clinical translation, and cross-functional product development.

• Design and analyze health studies using statistical and epidemiological methods to support decision-making
• Oversee research projects from design to dissemination
• Ensure quality of statistical analysis plans, data, analytical code, and outputs
• Work with Care Delivery, Product, and Commercial teams to demonstrate the effectiveness of Verily’s portfolio
• Develop metrics enabling strategic tracking based on evidence generation
• Design and conduct analyses of clinical outcomes, health care costs, and utilization, including KPIs and performance guarantees
• Collaborate with cross-functional teams to test service delivery models
• Evaluate the impact of new product features and AI on engagement and clinical outcomes

Staff Quantitative Scientist advancing Verily’s AI-enabled precision health analytics

Staff Quantitative Scientist

Staff Quantitative Scientist applying statistical and computational methods to Verily’s health data platform. Designing studies and evaluating healthcare outcomes, costs, utilization, products, and AI-enabled care solutions.

• performs research and/or development in collaboration with others
• makes detailed observations, analyzes data, and interprets results
• prepares technical reports, summaries, protocols, and quantitative analyses
• investigates, builds, and develops new methods and technologies for project advancement

Postdoctoral Scientist performing research and experiments at HHMI

Postdoctoral Scientist

Postdoctoral Scientist performing collaborative research and development in various scientific fields at HHMI. Analyzing data, preparing reports, and contributing to project advancement while fostering professional expertise.

• Proactively pursuing and performing process development studies for the purification of therapeutic proteins using MilliporeSigma technologies such as sterile, depth, tangential flow and virus filtration and chromatography.
• Involvement in filter selection and sizing, process optimization, and technology transfer activities associated with the purification of new pharmaceuticals
• Provide consultation to customers through email or teleconference calls.
• Collaborate and work with customer process development groups in the Midwest region.
• Work collaboratively with a team of local MilliporeSigma account managers to provide technical expertise to local customers.
• Adequately document customer interfacing activities.
• Communicate and work effectively in cross-functional teams, influence technical approaches, and support strategy execution.

Process Development Scientist developing purification processes for therapeutic proteins

Process Development Scientist

Process Development Scientist developing purification processes for therapeutic proteins at MilliporeSigma. Collaborating with global teams and providing technical expertise in a remote setting.

• Lead the design, development, and execution of phase-appropriate analytical methods in compliance with ICH and Health Authority guidelines.
• Perform release and stability testing on starting materials, intermediates and API for both development and GMP samples.
• Author and review technical documents including method qualification/validation/transfer protocols and reports for analytical procedures.
• Maintain and troubleshoot analytical instrumentation.
• Responsible for contributing to audit readiness and for participating in quality audits with FDA, other Regulatory Agencies, and customers, as needed.
• Ensures work in compliance with all state and federal regulations, including but not limited to GMP, DEA, FDA, etc.

Scientist Group Leader developing analytical methods for pharmaceutical ingredients

Scientist Group Leader

Scientist Group Leader developing analytical methods for pharmaceutical ingredients at Eurofins Scientific. Leading analytical development and ensuring compliance with regulatory guidelines.

• Provide expert support during pre- and post-sales activities, including scientific, technical, and application assistance.
• Deliver hands-on training by scheduling and managing demos, instrument installations, and customer onboarding sessions.
• Simplify complexity by presenting technical material in an engaging and accessible way, while professionally addressing questions or objections.
• Collaborate with the sales team to identify customer needs and demonstrate tailored product solutions.
• Assist customers with assay development, data analysis, and reporting to support their equipment purchase decisions.
• Monitor industry trends by maintaining knowledge of competitive products and emerging technologies.
• Advocate for customers by acting as the voice of the customer to internal teams and sharing valuable feedback about product performance and market needs.
• Build relationships by resolving inquiries, investigating complaints, and ensuring customer satisfaction.
• Contribute to market growth by supporting collaborations, preparing technical materials for seminars, and representing the company at scientific events and trade shows.

Field Application Scientist supporting biotech and pharmaceutical industries with expert instruments.

Field Applications Scientist

Field Application Scientist supporting biotech and pharmaceutical industries with Axion’s live cell analysis instruments. Engaging with customers during pre-sales and post-sales processes and providing expert technical assistance.

• Generate key research questions, then design and execute studies and analyses to address them
• Interpret study results and summarize insights across formats — documents, presentations, patent applications, and publications — for different audiences
• Leverage RGC and Regeneron datasets, external resources, and the scientific/medical literature to address research questions, weighing quantitative and qualitative strength of evidence
• Support target nomination and validation by applying RGC's human genetics capabilities alongside Regeneron's therapeutics platforms and development modalities
• Partner with Clinical Development to evaluate clinical-stage programs and identify opportunities for human genetics studies that inform indication selection or safety evaluation
• Participate in the intellectual life of the Cardiometabolic TAG, RGC, and Regeneron at large, helping build an inclusive culture where everyone can perform at their best
• Represent the Therapeutic Area Genetics team in cross-functional initiatives across RGC and Regeneron

Physician Scientist developing therapeutic targets in cardiometabolic genetics

Physician Scientist, Cardiometabolic Genetics

Physician Scientist developing therapeutic targets in cardiometabolic genetics at Regeneron. Engaging in research using human genetics and epidemiological insights to accelerate therapeutic development.

• The Sterility Assurance Scientist is responsible for supporting activities that maintain compliance to the applicable regulations (FDA, Canadian Medical Device Regulations (CMDR), European Medical Device Regulation (EU MDR), ISO 13485, and ISO 9001) as they apply to sterilization
• Maintains and revises procedures and methodologies to cover sterilization programs across sites
• Obtains and maintains knowledge of FDA, ISO, and EN sterilization and related microbiology standards and guidelines
• Supports EU MDR compliance by performing gap analysis and formulating gap resolution plans
• Monitors and ensures adequacy of contamination control measures at external suppliers
• Provides training to procedural changes
• Provides guidance and input on the resolution of sterility related non-conformances
• Creates and finalizes validation protocols and report ensuring they are clear, concise and compliant to work instructions and standards

Sterility Assurance Scientist ensuring compliance with sterilization regulations in healthcare

Senior Sterility Scientist

Sterility Assurance Scientist ensuring compliance across sterilization processes and methodologies in healthcare. Collaborating closely with various departments to maintain quality and regulatory standards.

• Supporting end‑to‑end Microbiological Quality & Sterility Assurance (MQ&SA) activities related to suppliers and external manufacturing processes
• Contributing to change requests and projects impacting controlled environments, cleaning, and sterilization processes
• Supporting contamination control strategies, including environmental monitoring and investigation activities
• Providing technical guidance and training on microbiological quality and sterility assurance
• Acting as subject matter expert for investigations, CAPA, non‑conformances, audit observations, and risk assessments
• Supporting due diligence activities (e.g., acquisitions, partnerships) by providing MQ&SA expertise and risk input
• Supporting development and updates of supplier quality agreements
• Coordinating and participating in supplier audits, including preparation, on‑site support, response review, and follow‑up activities
• Partnering with cross‑functional teams to support supplier qualification and lifecycle management
• Contributing to remediation activities following audits or regulatory findings
• Building strong relationships with external partners, including manufacturers, suppliers, sterilization providers, and testing laboratories

Microbiological Quality & Sterility Assurance Specialist at Johnson & Johnson

Senior Scientist – MQSA, Supplier/EM

Microbiological Quality & Sterility Assurance Specialist at Johnson & Johnson, supporting quality assurance activities for medical devices and pharmaceuticals in various locations.

• Invent synthetic routes and develop safe, robust, and cost-effective processes to manufacture synthetic and hybrid drug substances
• Advance enabling technologies to accelerate pharmaceutical development and to improve sustainability and process efficiency
• Support cGMP manufacturing and technology transfer to our internal manufacturing facilities and external contract manufacturers
• Ensure process performance through process understanding, modeling and characterization
• Contribute to drug substance development teams by providing experimental results, technical updates, documentation, data interpretation, recommendations, etc.
• Work cross-functionally to deliver regulatory documents and support regulatory filings
• Serve as a technical expert and keep current in the field of organic and process chemistry
• Work effectively in a multi-disciplinary team of chemists, engineers and attribute scientists
• Work independently in advancing projects and studies within required deadlines.

Senior Scientist in Process Development focusing on synthetic drug substances

Senior Process Development Scientist

Senior Scientist in Process Development working on synthetic and hybrid drug substances for patient care. Collaborating with cross-functional teams to ensure successful drug manufacturing processes.

• Evaluates DePuy Synthes medical device products and materials for biological safety per international medical device regulations and standards, GLP (Good Laboratory Practice) guidelines and internal procedures.
• Designs, initiates, coordinates, and interprets laboratory investigations for biocompatibility and toxicology studies for MD materials and products.
• Applies technical expertise to solve biocompatibility problems related to the ISO 10993 standards and regulatory authority requirements for product safety.
• Liaises with internal and cross-functional team members to review existing product documentation and coordinates, together with more senior staff, biocompatibility test strategies to ensure appropriate planning and execution of required testing and completion of relevant deliverables.
• Reviews, interprets, and summarizes testing data and ensures appropriate documentation and coordination of central documentation procedures required for risk assessment report completion.
• Interacts closely with and provides technical guidance and expertise to internal stakeholders (e.g., R&D, Clinical Affairs, Regulatory Affairs, Manufacturing, Quality Engineering, and Supplier Management).
• Can support regulatory/notified body requests as part of Audits and File/Product submissions/Reviews in applicable markets.
• Maintains effective communication of business-related issues or opportunities to next management level and if necessary, SMEs, via proper communication methods and/or tools.
• Identifies and evaluates potential risks and drives resolution with team members, peers, PMO and management.
• Participates in continuous improvement activities and actively participates in shaping processes and procedures.
• Responsible for communicating business related issues or opportunities to next management level.
• Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.
• For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable.
• Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.
• Performs other duties assigned as needed.

Scientist Biocompatibility supporting toxicity evaluation of medical devices

Biocompatibility Scientist

Scientist Biocompatibility at Johnson & Johnson evaluating biological safety of medical devices. Collaborating with cross-functional teams to ensure product compliance with regulations and standards.

Sr. Scientist supporting microbiological quality assurance processes in healthcare innovation

Sr. Scientist responsible for microbiological quality and sterility assurance for suppliers at Johnson & Johnson. Supporting investigations, audits, and quality agreements in the medical device industry.

Scientist role in Microbiological Quality and Sterility Assurance at Johnson & Johnson

Scientist role supporting Microbiological Quality and Sterility Assurance at Johnson & Johnson. Collaborating on contamination control and supplier audits across several locations in the U.S.

• Analyze and characterize materials and their chemical composition and behavior
• Understand interactions between raw materials and packaging (tubes, bottles, etc.)
• Assess how supplier differences impact material performance and product quality
• Investigate material-related issues and drive practical, science-based solutions
• Collaborate closely with cross-functional teams across Product Science, MS&T, and Quality
• Translate complex findings into clear technical documentation and presentations

Material Scientist optimizing materials in dermatology company

Material Scientist

Material Scientist analyzing and characterizing materials for dermatological products. Collaborating with cross-functional teams to drive science-based solutions and optimize product performance.

• Lead customer engagement and technical delivery by preparing and delivering LC/MS product demonstrations, proteomics workflows, training, and ongoing application support to drive customer success and adoption
• Drive commercial impact and market growth by partnering with sales and business teams to identify opportunities, align application strategies, and influence customer decisions across key market segments
• Develop and advance proteomics solutions by designing and implementing end-to-end workflows, including sample preparation, analytical methods, and data processing approaches
• Support product innovation and portfolio expansion by contributing to the definition, testing, and application of new hardware and software solutions across nominal and accurate mass LC-MS technologies
• Act as a scientific thought leader and brand ambassador by building a strong presence in the proteomics community, representing SCIEX at conferences, and influencing stakeholders across scientific, commercial, and executive audience

Senior Application Scientist providing technical support in proteomics at SCIEX

Senior Application Scientist – Proteomics

Senior Application Scientist responsible for LC-MS product demonstrations and applications support in life sciences. Leading customer engagement and driving scientific solutions in a collaborative environment.

• Provide pre-, peri-, and post-sales technical support to customers through live demonstrations, troubleshooting inbound customer questions/issues, proactive engagement with customers, and collecting feedback for product development, supporting operations communications, aligning shipments, diagnosing technical issues, and doing basic preventative maintenance on instrumentation.
• Demonstrate the value of ONI’s technology suite to potential customers through in-person demonstrations at customer sites across multiple application spaces
• Deliver high-quality customer experience by maintaining cutting-edge imaging method expertise, operating as a peer to customers
• Create product awareness by engaging with the scientific community, answering technical questions, delivering presentations and demonstrations to showcase ONI’s products at conferences, webinars, seminars, and other industry events
• Work closely with the Sales team to understand the status and details of each opportunity in the sales funnel, and providing scientific insights during pitches and meetings with potential customers
• Design and conduct experiments at customer’s sites or in ONI’s laboratory, to highlight how ONI’s technology suite can solve specific challenges and meet their needs
• Assist customers in the setup and operation of products by conducting demonstrations and training sessions, both remotely and on-site, to ensure customers can effectively utilize ONI’s products
• Provide ongoing hands-on support and guidance to customers, serving as a primary point of contact for technical inquiries, support requests, troubleshooting, and issue resolution
• Facilitate the packing & shipping of components, instruments and products to customer base and internal users using couriers
• Work with global logistics team to coordinate shipments and liaise with external and internal customers on a daily basis
• Maintain accurate records of customer interactions, demonstration outcomes, technical issues, and resolutions in Salesforce
• Generate regular reports on customer feedback, product performance, and customer success metrics for Product and Marketing teams to assess and improve customer satisfaction

Field Application Scientist providing technical support for life science technology

Field Application Scientist

Field Application Scientist providing pre-, peri-, and post-sales technical support for ONI’s life science innovations. Engaging with customers through demonstrations, training, and troubleshooting.

• Provide quantum solutions to ensure scientific and commercial success
• Provide application-specific customer support, including onsite system integration
• Maintain and establish customer contacts to secure future sales and support market growth
• Represent Zurich Instruments at trade shows, engage with opinion leaders and work with leading quantum researchers across the US
• Produce marketing material, including presentations, product documentation, and videos

Application Scientist in quantum computing at Zurich Instruments

Application Scientist – Quantum Technologies

Application Scientist in quantum technologies at Zurich Instruments. Joining the marketing and sales team to provide quantum solutions and customer support in Boston.

Scientist jobs in Massachusetts

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Staff Preclinical Scientist

Staff Quantitative Scientist

Postdoctoral Scientist

Process Development Scientist

Scientist Group Leader

Field Applications Scientist

Physician Scientist, Cardiometabolic Genetics

Senior Sterility Scientist

Senior Scientist – MQSA, Supplier/EM

Senior Process Development Scientist

Biocompatibility Scientist

Senior Scientist – MQSA, Supplier/EM

Senior Scientist – MQSA, Supplier/EM

Material Scientist

Senior Application Scientist – Proteomics

Field Application Scientist

Application Scientist – Quantum Technologies